The Anspach Effort recalls
The Anspach Effort appears in 261 official U.S. recall notices indexed by RecallRadar.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the Pneumatic Motor Systems including: BlackMax Motor Systems, Micr…
FDA Device · Class II · 2013-11-20 · The Anspach Effort - Cutting Bur Chart (part number 20-0019) utilized with the Electric and Pneumatic Motor Systems including: MicroMax Motor Systems, XMax Moto…
FDA Device · Class II · 2013-11-20 · The Anspach Effort - ***REF SC2100***eMax 2 Plus Console***SN G 10307653002*** Product Usage: The RPM of the Motor Handpiece may be less than 80,000 RPM (approx…
FDA Device · Class II · 2013-07-10 · The Anspach Effort - ***REF SC2102***eMax 2 Plus Console, Single Port, no Irrigation***SN G16307882402*** Product Usage: The eMax console is intended to operate…
FDA Device · Class II · 2013-07-10 · The Anspach Effort - ***REF SC2101***eMax 2 Plus Console, Single Port, with Irrigation***SN G17307901802*** Product Usage: The RPM of the Motor Handpiece may be…
FDA Device · Class II · 2013-07-10 · The Anspach Effort - ***REF S-3D*** 3mm Diamond Ball
FDA Device · Class II · 2013-06-05 · The Anspach Effort - Anspach Effort, Inc., 98-0061 MA-15C Bearing Sleeve with Removable Bur Guard
FDA Device · Class II · 2013-02-13 · The Anspach Effort - "***Electric Systems Foot Control with Direction Only***Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine an…
FDA Device · Class II · 2012-10-24 · The Anspach Effort - "***Electric Systems Foot Control****Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium
FDA Device · Class II · 2012-10-24 · The Anspach Effort - "***Electric Systems Foot Control with Direction and Irrigation***Rx Only***" Product Usage: Cutting and shaping bone including bones of th…
FDA Device · Class II · 2012-10-24 · The Anspach Effort - .***ANSPACH***Sterile
FDA Device · Class II · 2012-08-01 · The Anspach Effort